Shi Yonglin, Wang Xian, Chen Guoping, Zhang Jin, Hu Wanfu
Bing Du Xue Bao. 2015 Nov;31(6):660-4.
To study on the phylogenetic characterization of the VP1 genes of coxsackievirus A16 (CVA16) causing hand-food-mouth disease (HFMD) isolated from Anhui province in 2014. A total of 413 throat swab specimens from HFMD patients were collected during January to November, 2014 for the isolation and identification of enteroviruses using real-time RT-PCR assays. The VP1 regions of CVA16 isolates were amplified using RT-PCR and sequenced. And the phylogenetic tree was constructed among the VP1 regions of those isolates, the different genotypes and sub-genotypes of CVA16 strains. A total of 97 enteroviruses were isolated from 413 samples, the positive rate was 23.49% (97/413), including seventeen CVA16, seventy six HEV71 and four other enteroviruses. The results of the phylogenetic tree showed that 17.CVA16 strains isolated from Anhui in 2014 clustered within B1b evolution branch of B1 genotype. The nucleotide and amino acid sequence identities were 95.30%-100% and 98.70%-100% among the isolates, respectively, but within B1b branch of 17 strains formed several small transmission chains. The nucleotide acid of 17 CVA16 isolates in Anhui province were closed to the strains isolated from Yunnan, Hunan, Guangdong, Tibet and Jiangsu, especially from Hunan in 2013 and from Shenzhen of Guangdong in 2014, the identity were 96.40%-99.70%. The CVA16 strains isolated from Anhui in 2014 were all belong to genetic subtype B1b of B1 genotype was dominant, and among those isolates, several small virus transmission chains had formed with co-circulating and evolution.
研究2014年从安徽省分离出的引起手足口病(HFMD)的柯萨奇病毒A16(CVA16)VP1基因的系统发育特征。2014年1月至11月期间,共收集了413份手足口病患者的咽拭子标本,采用实时RT-PCR检测法进行肠道病毒的分离和鉴定。使用RT-PCR扩增CVA16分离株的VP1区域并进行测序。并在这些分离株的VP1区域、CVA16毒株的不同基因型和亚基因型之间构建系统发育树。从413份样本中共分离出97株肠道病毒,阳性率为23.49%(97/413),其中包括17株CVA16、76株HEV71和4株其他肠道病毒。系统发育树结果显示,2014年从安徽分离出的17株CVA16毒株聚集在B1基因型的B1b进化分支内。分离株之间的核苷酸和氨基酸序列同一性分别为95.30%-100%和98.70%-100%,但在17株的B1b分支内形成了几个小的传播链。安徽省17株CVA16分离株的核苷酸与从云南、湖南、广东、西藏和江苏分离出的毒株相近,特别是与2013年从湖南和2014年从广东深圳分离出的毒株,同一性为96.40%-99.70%。2014年从安徽分离出的CVA16毒株均属于B1基因型的遗传亚型B1b,且在这些分离株中,随着共同循环和进化形成了几个小的病毒传播链。